Canonical Allele Identifier: PA645378037
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359686
ClinVar RCV Id: RCV000262624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Glu4125Asp
CA10623643
NM_001277115.2:c.12375G>C
CA366964228
NM_001277115.2:c.12375G>T